Naproxen Sodium NDC 0363-7510

NDC codes

FDA NDC Directory

Product NDC (as listed)0363-7510Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00363-7510Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package
0363-7510-20	00363751020	1 BOTTLE, PLASTIC in 1 BOX (0363-7510-20) / 20 TABLET in 1 BOTTLE, PLASTICMarketed from Jan 31, 2020
0363-7510-40	00363751040	1 BOTTLE, PLASTIC in 1 BOX (0363-7510-40) / 40 TABLET in 1 BOTTLE, PLASTICMarketed from Jan 31, 2020
0363-7510-50	00363751050	1 BOTTLE, PLASTIC in 1 BOX (0363-7510-50) / 50 TABLET in 1 BOTTLE, PLASTICMarketed from Jan 31, 2020
0363-7510-80	00363751080	1 BOTTLE, PLASTIC in 1 BOX (0363-7510-80) / 80 TABLET in 1 BOTTLE, PLASTICMarketed from Jan 31, 2020

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Naproxen Sodium
Generic name (nonproprietary): naproxen sodium
Active ingredients: Naproxen sodium — 220 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Walgreens
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 202807
Marketing start: Jan 31, 2020
Listing expires: Dec 31, 2026
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers: Product ID 0363-7510_e5a5fe51-e1a2-4103-b1f5-2a2d33e79307SPL ID e5a5fe51-e1a2-4103-b1f5-2a2d33e79307SPL set ID a380cace-43dc-4b9c-84d3-0b38241d9d2eUNII 9TN87S3A3CUPC 0311917031033
Pharmacologic class: Nonsteroidal Anti-inflammatory Drug

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N400363751020 followed by a unit qualifier and the quantity

Package 00363-7510-20. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Mar 30, 2022.

Indications (excerpt from the label)

Uses temporarily relieves minor aches and pains due to: minor pain of arthritis muscular ache backache menstrual cramp headache toothache the common cold temporarily reduces fever

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 202807

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 202807
Product	Strength	Form · route	Labeler	Product NDC
Naproxen Sodium	Naproxen sodium 220 mg/1	CapsuleOral	P & L Development, LLC	59726-751